Linked Data
dbSNP Id:
rs1557007362
gnomAD v2:
X-48547469-G-T
gnomAD v4:
X-48689080-G-T
MyVariant Identifiers:
chrX:g.48547469G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48689080G>T , CM000685.2:g.48689080G>T | GRCh38 |
| NC_000023.10:g.48547469G>T , CM000685.1:g.48547469G>T | GRCh37 |
| NC_000023.9:g.48432413G>T | NCBI36 |
| NG_007877.1:g.10284G>T , LRG_125:g.10284G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474174.2:n.582+14G>T | ||
| ENST00000698625.1:c.1338+14G>T | ENSP00000513844.1:n.1338+14G>T | |
| ENST00000698626.1:c.1338+14G>T | ENSP00000513845.1:n.1338+14G>T | |
| ENST00000698635.1:c.1338+14G>T | ENSP00000513850.1:n.1338+14G>T | |
| ENST00000376701.5:c.1338+14G>T MANE Select | ENSP00000365891.4:n.1338+14G>T | |
| ENST00000376701.4:c.1338+14G>T | ENSP00000365891.4:n.1338+14G>T | |
| ENST00000470107.1:n.47+14G>T | ||
| NM_000377.2:c.1338+14G>T , LRG_125t1:c.1338+14G>T | NP_000368.1:n.1338+14G>T | |
| XM_011543977.1:c.1182+14G>T | XP_011542279.1:n.1182+14G>T | |
| XM_011543977.2:c.1182+14G>T | XP_011542279.1:n.1182+14G>T | |
| XM_017029786.1:c.1338+14G>T | XP_016885275.1:n.1338+14G>T | |
| NM_000377.3:c.1338+14G>T MANE Select | NP_000368.1:n.1338+14G>T |